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Hemoglobin
international journal for hemoglobin research
Volume 29, 2005 - Issue 3
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Original Article

Hyperbilirubinemia in Homozygous HbE Disease Is Associated with the UGT1A1 Gene Polymorphism

Eunice Sindhuvi Edison Department of Haematology, Christian Medical College, Vellore, India
,
Ramachandran V. Shaji Department of Haematology, Christian Medical College, Vellore, India
,
Alok Srivastava Department of Haematology, Christian Medical College, Vellore, India
&
Mammen Chandy Department of Haematology, Christian Medical College, Vellore, IndiaCorrespondence[email protected]
, F.R.C.P.A. , M.D. , F.R.A.C.P.
Pages 189-195 | Received 07 Mar 2005, Accepted 23 Mar 2005, Published online: 07 Jul 2009

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Read on this site (2)

Divya Jayasree, Ramachandran V. Shaji, Biju George, Vikram Mathews, Alok Srivastava & Eunice S. Edison. (2016) Clinical, Hematological and Molecular Analysis of Homozygous Hb E (HBB: c.79G > A) in the Indian Population. Hemoglobin 40:1, pages 16-19.
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Pooja S. Dabke, Roshan B. Colah, Kanjaksha K. Ghosh & Anita H. Nadkarni. (2014) Role of co-inherited Gilbert syndrome on hyperbilirubinemia in Indian beta thalassemia patients. Hematology 19:7, pages 388-392.
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Articles from other publishers (2)

Pratibha DhimanPriyanka SaxenaChhagan BihariArchana RastogiS.K Sarin. (2015) New approaches for cholestasis in hemoglobinopathies. Blood Research 50:2, pages 118.
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Khushnooma Y. Italia, Farah F. Jijina, Dipty Jain, Rashid Merchant, Anita H. Nadkarni, Malay Mukherjee, Kanjaksha Ghosh & Roshan B. Colah. (2010) The effect of UGT1A1 promoter polymorphism on bilirubin response to hydroxyurea therapy in hemoglobinopathies. Clinical Biochemistry 43:16-17, pages 1329-1332.
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